Proton conducting materials

ABSTRACT

Materials are provided that may be useful as ionomers or polymer ionomers, including compounds including bis sulfonyl imide groups which may be highly fluorinated and may be polymers.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional application of prior application Ser.No. 13/269,907, filed Oct. 10, 2011, now allowed, which is a divisionalof U.S. application Ser. No. 12/429,371, filed Apr. 24, 2009, whichclaims the benefit of U.S. Provisional Patent Application No.61/047,643, filed Apr. 24, 2008, the disclosure of which is incorporatedby reference in its entirety herein.

GOVERNMENT RIGHTS

This disclosure was made with Government support under CooperativeAgreement DE-FG36-07GO17006 awarded by DOE. The Government has certainrights in this disclosure.

FIELD OF THE DISCLOSURE

This disclosure relates to materials that may be useful as ionomers orpolymer ionomers.

BACKGROUND OF THE DISCLOSURE

In some applications, including some automotive applications, there is adesire to operate fuel cells at higher temperatures, e.g., in theneighborhood of 120° C., in part for the purpose of simplifying thecooling systems while improving the heat rejection. Higher temperaturesmay also provide efficiency gains in using the waste heat in combinedheat and power systems. Operating at higher temperatures may alsoimprove catalyst resistance to CO poisoning when using reformed fuels.In some applications, humidifying incoming reactant gas streams has beenpracticed in order to elevate the level of hydration in the protonexchange membrane (PEM), however, humidifiers add to the initial cost ofa system and increase parasitic power losses during operation.Humidifying become increasingly difficult at elevated temperatures;hence there is a need for inherently higher-conducting materials toefficiently move protons with little or no water.

SUMMARY

Briefly, the present disclosure provides compounds according to theformula:(R¹—O—)₂—P(═O)_(m)—Ar—SO₂NH—SO₂—R²

wherein each R¹ is independently chosen from the group consisting ofhydrogen, alkyl, alkylene or aryl groups which may contain heteroatomsand which may be substituted, polymers, metals, metal oxides, metalphosphates, metal phosphonates and inorganic particles, wherein m is 0or 1, wherein Ar is an aromatic group which may include heterocycles andpolycycles and may be substituted, and wherein R² is chosen from thegroup consisting of alkyl, alkylene or aryl groups which may containheteroatoms and which may be substituted, and polymers. In someembodiments, Ar is phenylene. In some embodiments, Ar is phenylene-R³,wherein R³ is chosen from the group consisting of hydrogen, alkyl,alkylene or aryl groups which may contain heteroatoms and which may besubstituted, and polymers. In some embodiments, R² is a fluoropolymer.In some embodiments, R² is substituted with one or more acid groupsselected from the group consisting of sulfonic acid groups andphosphonic acid groups.

In another aspect, the present disclosure provides compounds accordingto the formula:

wherein R¹ is chosen from the group consisting of metals, metal oxides,metal phosphates, metal phosphonates and inorganic particles, wherein mis 0 or 1, wherein Ar is an aromatic group which may includeheterocycles and polycycles and may be substituted, and wherein R² ischosen from the group consisting of alkyl, alkylene or aryl groups whichmay contain heteroatoms and which may be substituted, and polymers. Insome embodiments, Ar is phenylene. In some embodiments, Ar isphenylene-R³, wherein R³ is chosen from the group consisting ofhydrogen, alkyl, alkylene or aryl groups which may contain heteroatomsand which may be substituted, and polymers. In some embodiments, R² is afluoropolymer. In some embodiments, R² is substituted with one or moreacid groups selected from the group consisting of sulfonic acid groupsand phosphonic acid groups. In some embodiments, one or more or every R¹is a metal or metal oxide wherein the metal is selected from the groupconsisting of Zr, Ti, Th and Sn. In some embodiments, one or more orevery R¹ is a metal or metal oxide wherein the metal is selected fromthe group consisting of tetravalent metals.

In another aspect, the present disclosure provides compounds accordingto the formula:R¹ _(n)—Ar—SO₂NH—SO₂—R²

wherein each R¹ is independently chosen from the group consisting ofhydrogen, alkyl, alkylene or aryl groups which may contain heteroatomsand which may be substituted, polymers, metals, metal oxides, metalphosphates, metal phosphonates and inorganic particles, wherein n is 1,2 or 3, wherein Ar is an aromatic group which may include heterocyclesand polycycles and may be substituted, and wherein R² is chosen from thegroup consisting of alkyl, alkylene or aryl groups which may containheteroatoms and which may be substituted, and polymers. In someembodiments, Ar is phenylene. In some embodiments, Ar is phenylene-R³,wherein R³ is chosen from the group consisting of hydrogen, alkyl,alkylene or aryl groups which may contain heteroatoms and which may besubstituted, and polymers. In some embodiments, R² is a fluoropolymer.In some embodiments, R² is substituted with one or more acid groupsselected from the group consisting of sulfonic acid groups andphosphonic acid groups.

In another aspect, the present disclosure provides polymer electrolytescomprising a highly fluorinated backbone and first pendant groups whichcomprise groups according to the formula:—SO₂—NH—SO₂—ArA_(n)

wherein Ar is an aromatic group of 5-24 carbon atoms which may includeheterocycles and polycycles and may be substituted, where A is selectedfrom the group consisting of —SO₃H and —PO₃H₂, where n is between 1 andq, where q is one-half the number of carbons in Ar. In some embodimentsthe polymer electrolyte comprises a perfluorinated backbone. In someembodiments the polymer electrolyte comprises second pendant groupswhich comprise groups according to the formula: —SO₃H. In someembodiments the ratio of first to second pendant groups is p, where p isbetween 0.01 and 100, between 0.1 and 10, between 0.1 and 1 or between 1and 10.

In another aspect, the present disclosure provides polymer electrolytemembranes or membrane electrode assemblies comprising the presentpolymer electrolytes, which may additionally comprising a porous supportor may additionally be crosslinked.

In this application:

“equivalent weight” (or “EW”) of a polymer means the weight of polymerwhich will neutralize one equivalent of base (allowing that, wheresulfonyl halide substituents or other substituents that would beconverted into acidic functions during use of the polymer in a fuel cellare present, “equivalent weight” refers to the equivalent weight afterhydrolyzation of such groups);

“highly fluorinated” means containing fluorine in an amount of 40 wt %or more, typically 50 wt % or more and more typically 60 wt % or more;and

“substituted” means, for a chemical species, substituted by conventionalsubstituents which do not interfere with the desired product or process,e.g., substituents can be alkyl, alkoxy, aryl, phenyl, halo (F, Cl, Br,I), cyano, nitro, etc.

DETAILED DESCRIPTION

This disclosure relates to production of materials, including polymers,particles and small molecules, linked to acid-containing through thecovalent bonding of materials using sulfonamide, bis sulfonyl imide andphosphonic linkages.

In another aspect, this disclosure concerns fuel cell membrane materialswith an increased number of strong acid groups created in someembodiments by reaction of these acid containing molecules with acidcontaining organic molecules, metal oxide or phosphate particles, metalsalts, heteropolyacids, and the like.

Another aspect of this disclosure involves the use of thesemultifunctional materials to develop crosslinked structures for improvedmechanical properties or to minimize component leaching.

Materials taught in this disclosure may be used for fuel cellapplications such as in the manufacture of proton exchange membranes(PEM), as catalyst additives or in tie layers designed to be thermallyand chemically robust while operating within a fuel cell's harshenvironment at higher temperatures and to conduct protons, withsignificantly higher levels of bound acidic groups, while in a lowhydration state.

This disclosure describes the modification of PFSA's or other polymersby the conversion of the sulfonic acid group to a bis sulfonyl imidegroup with an aromatic group which can be further modified by theattachment of additional acid groups (for improved conductivity) orphosphonic acid groups or silane groups (for attachment ofheteropolyacids, for the attachment of inorganic particles such aszirconia or zirconyl phosphate or for the attachment of silicaparticles).

This group can also be used to create cross-links. Crosslinking may beaccomplished thru the use of difunctional reactants. Examples includebut are not limited to: ammonia, benzene disulfonyl chloride,naphthalene disulfonyl chloride sulfonic acid sodium salt,bis-(phenyldisulfonyl anhydride) and disulfonamides (e.g. benzenedisulfonamide).

Below are two schematics detailing possible linking reactions

Useful reactive groups include halides, sulfonyl halides, disulfonylanhydrides, sulfonamides, amines, phosphonic diols, acids and esters,Tungstenic diols, and the like.

Aromatic groups may be sulfonated by any suitable method. Aromaticgroups may be sulfonated by use of Na₂SO₃, chlorosulfonic acid,trimethyl silyl sulfonic acid, sulfuric acid, or other sulfonatingagents.

This disclosure further describes the attachment of small moleculescontaining bis sulfonyl imides to inorganic moieties such as HPA's orparticles and methods of synthesizing these compounds.

This disclosure incorporates by reference the disclosures of U.S. patentapplication Ser. No. 12/342,370, filed Dec. 23, 2008, U.S. Pat. No.7,285,349, issued Oct. 23, 2007, U.S. Pat. No. 7,348,088, issued Mar.25, 2008, U.S. Pat. No. 6,727,386, issued Apr. 27, 2004, U.S. Pat. No.6,863,838, issued Mar. 8, 2005, and U.S. Pat. No. 6,090,895, issued Jul.18, 2000.

Polymers according to the present disclosure may be crosslinked by anysuitable method, which may include methods disclosed in U.S. Pat. No.7,179,847, issued Feb. 20, 2007; U.S. Pat. No. 7,514,481, issued Apr. 7,2009; U.S. Pat. No. 7,265,162, issued Sep. 4, 2007; U.S. Pat. No.7,074,841, issued Jul. 11, 2006; U.S. Pat. No. 7,435,498, issued Oct.14, 2008; U.S. Pat. No. 7,259,208, issued Aug. 21, 2007; U.S. Pat. No.7,411,022, issued Aug. 12, 2008; U.S. Pat. No. 7,060,756, issued Jun.13, 2006; U.S. Pat. No. 7,112,614, issued Sep. 26, 2006; U.S. Pat. No.7,060,738, issued Jun. 13, 2006; U.S. Pat. No. 7,173,067, issued Feb. 6,2007; and U.S. Pat. No. 7,326,737, issued Feb. 5, 2008; the disclosuresof which are incorporated herein by reference.

The scope of this disclosure should not be restricted solely to polymerselectrolytes or fuel cell applications, as one could envisionapplications outside of fuel cell use.

Objects and advantages of this disclosure are further illustrated by thefollowing examples, but the particular materials and amounts thereofrecited in these examples, as well as other conditions and details,should not be construed to unduly limit this disclosure.

EXAMPLES

Unless otherwise noted, all reagents were obtained or are available fromAldrich Chemical Co., Milwaukee, Wis., or may be synthesized by knownmethods.

Example 1 Sulfonamide-Functional Polymer

A sulfonamide functional polymer was created by reacting a polymerhaving pendent sulfonyl fluoride groups with ammonia followed by ionexchange, as diagrammed below. As indicated, a side reaction can occurinvolving formation of imide crosslinks by the reaction of thesulfonamide with a second —SO₂F group.

The polymer used was a copolymer of tetrafluoroethylene (TFE) andFSO₂—CF₂CF₂CF₂CF₂—O—CF═CF₂, described in U.S. patent application Ser.Nos. 10/322,254, 10/322,226 and 10/325,278, which are incorporatedherein by reference. About 23 g of a 90/10 blend of a ˜680 EW polymerand an 800 EW polymer was placed into a 600 ml Parr bomb with 150 gacetonitrile. The bomb was sealed up, evacuated and with low agitationchilled to −20 C. Ammonia was added to 40 psig and the temperature keepbelow 5 C for 6 hours. It was then allowed to warm up to roomtemperature overnight.

The vessel was opened and the grey solid polymer separated and dissolvedin 108 g of methanol and 20 g of DI water with modest warming.

5.7 g of lithium hydroxide monohydrate and 40 g of DI water was added tothe clear colorless solution and roller mixed with modest heating.

The solution was then exposed to acidified and rinsed Amberlite IR-120ion exchange beads a total of 6 times to drop the solution pH containingpolymer to ˜3. An NMR spectrum of the lower pH solution shows asubstantial sulfonamide peak at −115.0 with a small sulfonic acid peakat −115.7, with a peak integration ratio of 12 to 1. The solution wasdried at 60 C, overnight, resulting in 12.1 g of light yellow solid. Thepolymer was then redissolved in acetonitrile, allowed to stand andsettle. The dissolved portion was again coated out and dried, resultingin 8.7 g of slightly yellow, slightly cloudy, rigid film.

Example 2

1.51 g of the sulfonamide functional perfluorinated polymer from Example1 was dissolved in 13.7 g of dry acetonitrile. 0.85 g of4-Bromobenzenesulfonyl chloride was added and quickly dissolved. Thevial was cooled to −10 C and 1.11 g of triethylamine added and stirred.The vial was heated at 70 C for 2 hours in an oil bath. An additional0.49 g of triethylamine was added after 2 hours. A 6% H₂SO₄ in watersolution was used to lower the pH from ˜10 to ˜3. In doing so, thecloudy polymer precipitated out. This solid was redissolved quickly inacetonitrile and additional 6% H₂SO₄ in water solution used to drop pHto ˜0.5, with triethylamine used to bring the pH back to ˜2.5.Tetrahydrofuran was added in hopes of reprecipitating the polymerwithout success. The solution was dried down at 65 C for 3 hours,without the fine material which had settled to the bottom. 1.6 g oflight tan film was recovered and an NMR spectrum showed a substantialbis sulfonylimide peak at −113.5, with no sulfonamide peak at ˜−115.0and a small sulfonic acid peak at −115.5, with a peak integration ratioof 11 to 1.

Example 3

1 gm of fluoropolymer containing phenylbromide attached to the polymervia a bis sulfonylimide group, obtained in Example 2, was suspended in30 ml EtOH. To this was added 49 mg of Palladium(II) acetate and 173 mgof triphenylphosphine followed by dropwise addition of 0.35 ml ofN,N-dicyclohexylmethylamine and 0.225 ml of diethyl phosphite. Thereaction mixture was heated for 30 min at 70° C. In order, to dissolvethe polymer 4 ml of N-methyl pyrrolidone was added. A clear formed, wasrefluxed for 15 hours at 80° C. The solvent was removed in a rotaryevaporator. The product obtained shows a 31P NMR signal at δ 16.2 ppm(referenced to H₃PO₄) confirming the formation of the phosphonate ester.

Example 4 bis phosphophenyl bis sulfonyl imide acid

Step 1. 23.6 gm of 4-Bromobenzenesulfonamide was added to 100 ml of dryAcetonitrile in a three-necked round bottom flask. The flask was cooledto 0° C. and a water cooled reflux condenser was attached to the centerneck of the flask. The flask was continuously purged with Nitrogenduring the course of the reaction. 30.3 gm of Triethylamine was added tothe flask under stirring. 25.6 gm of 4-Bromobenzenesulfonylchloride wasweighed in a Nitrogen purged box and added in portions to the flaskunder constant stirring. 30 ml of acetonitrile was added to the mixtureto wash any residual 4-bromobenzenesulfonyl chloride sticking to theneck of the round bottom flask. The mixture was stirred for ˜24 hours.The triethylamine hydrochloride salt was filtered and the filtrate wasconcentrated to yield the brown triethylamine salt of the bis sulfonylimide product in ˜50% yield. The formation of bis sulfonyl imide productwas confirmed by ¹H NMR and ¹³C NMR.

Step 2. An oven dried flask was cooled under nitrogen and charged with 1gm of product from step 1, palladium(II) acetate (8 mg) andtriphenylphosphine (30 mg). 15 ml of Ethanol was introduced into theflask through a needle and syringe followed by dropwise addition ofN,N-dicyclohexylmethylamine (1.25 ml) and diethyl phosphite (0.61 ml).The reaction mixture was refluxed for 15 hours at 80° C. The solvent wasremoved in a rotary evaporator to obtain the product as triethyl aminesalt—a brown semisolid in 80% yield. The phosphonation was confirmed by³¹P NMR signal at δ 16.74 ppm (referenced to H₃PO₄).

Step 3. 1 g of step 2 product was refluxed with 20 ml of 12N HCl for 36hours to hydrolyze the phosphonate ester. The resulting mixture wasdried using a rotary evaporated to yield the hydrolyzed phosphonic acidproduct. The completion of the hydrolysis of the diethylphosphonateester was confirmed by the absence of the ethyl signals at 3.99 ppm,1.22 ppm in the final product and by the ³¹P NMR: δ 12.06 ppm(referenced to H₃PO₄).

Example 5 (4-benzenebisulfonimide-phenyl)-phosphonic acid

Step 1: (4-sulfamoyl-phenyl)-phosphonic acid diethyl ester

An oven dried flask was charged with 6.5 gm of4-bromobenzenesulphonamide, 112.2 mg of palladium(II) acetate and 392.5mg of triphenylphosphine. 100 ml of Ethanol was introduced into theflask through a needle and syringe followed by dropwise addition of 8 mlN,N-dicyclohexylmethylamine and 3.87 ml of diethyl phosphite. Thereaction mixture was refluxed for 15 hours at 80° C. On cooling, slowprecipitation of the product as a white solid is observed. The volume ofsolvent was reduced to half in a rotary evaporator and the solidprecipitate was filtered through a sintered funnel under vacuum. Theproduct was obtained as a white solid in 80% yield. ³¹P NMR: δ 15.83 ppm(referenced to H₃PO₄), ¹⁵N NMR: δ 95.5 ppm (referenced to liquid ammoniaas 0 ppm through a secondary reference of glycine),

Step 2: (4-benzenedisulfonimide-phenyl)-phosphonic acid diethyl ester

An oven dried flask was charged with 2.5 g of(4-sulfamoyl-phenyl)-phosphonic acid diethyl ester (Product from step 1)and 100 ml of acetonitrile. The flask was cooled to 0° C. and to it 3.2ml of benzene sulfonyl chloride was added dropwise followed by 8.5 ml oftriethylamine. The reaction was stirred for 3 hours and triethyl aminehydrochloride salt was filtered off. Lithium salt of the product wasobtained by adding 10 g of LiOH.H₂O to the reaction mixture. The solidswere filtered and the filtrate concentrated to yield the product in 80%yield. ³¹P NMR: δ 16.8 ppm (referenced to H₃PO₄).

Step 3: (4-benzenedisulfonimide-phenyl)-phosphonic acid

18 g of product from step 2 was refluxed with 200 ml of 12N HCl for 36hours to hydrolyze the phosphonate ester. The resulting mixture wasdried using a rotary evaporated to yield the hydrolyzed phosphonic acidproduct in 95% yield. The completion of the hydrolysis of thediethylphosphonate ester was confirmed by the absence of the ethylsignals from the ester at 4.02 ppm and 1.23 ppm, ³¹P NMR: δ 11.36 ppm(referenced to H₃PO₄). The lithium free product was obtained by ionexchange on strongly acidic type amberlite resin column.

Example 6 Zr(O₃P—C₆H₄—SO₂NHSO₂—C₆H₅)₂

0.5 gm of ZrOCl₂.8H₂O was dissolved in 30 gm of deionized water in aPolypropylene bottle. To this solution 2 gm of (50 wt %) Hydrofluoricacid was added under stirring. After 5 min 1.3 gm of phosphonic acidH₂O₃P—C₆H₄—SO₂NHSO₂—C₆H₅ synthesized in Example 5 was added to the abovemixture. The polypropylene bottle containing the mixture was heated inan oil bath under stirring at 80° C. for 16 hours. The dried product waswashed with methanol and centrifuged. The supernatant was decanted. Theprecipitate was dried in a hot air oven at 110° C. for 15 minutes. X-raydiffraction shows peaks for a layered the zirconium phosphonates solid(001 reflection at 23.5 Å, 002 reflection at 11.7 Å and 003 reflectionat 7.85 Å).

Example 7 Prophetic

The phosphonic acid synthesized in Example 5 is attached to a lacunaryheterpolyacid, such as described in U.S. patent application Ser. No.12/266,932, filed Nov. 7, 2008, (the disclosure of which is incorporatedherein by reference), by reacting the phosphonic acids with a lacunaryheteropolyacid salt by the method described in Example 6.

Example 8 Perfluorinated Polymer with Side Chains According to theFormula: —O—(CF₂)₄—SO₂—NH—SO₂-PhF₅

10 g of a substantially sulfonamide-functional polymer at 10% solids,made according to the process of Example 1 using 733 EW polymer, and 5.6g of pentafluorobenzenesulfonyl chloride (from Alfa Aesar, Ward Hill,Mass., USA) were dissolved in 45 ml of Aldrich sealed acetonitrile. Theaddition was done under nitrogen. After allowing the mixture to stir for1 hr, at this time all solids have dissolved in the solution, 4.25 g ofAldrich sealed triethyl amine was added to the mixture and allowed tostir for 2 hr followed by mild heating (72° C.) for an additional 15min. Sample from the crude mixture was analyzed with NMR. The fluorineNMR shows a strong peak at −113.4 ppm which corresponds to the CF₂ groupadjacent to the sulfur in the pentafluorosulfonylimide of the polymer.

Example 9 Perfluorinated Polymer With Side Chains According to theFormula: —O—(CF₂)₄—SO₂—NH—SO₂-PhF₂

The reaction described in Example 8 was carried out using 2 g of3,5-difluorobenzenesulfonyl chloride (from Alfa Aesar, Ward Hill, Mass.,USA) and 10 g of polymer at 10% solids in 45 ml of acetonitrile.

Example 10 Perfluorinated Polymer with Side Chains According to theFormula: —O—(CF₂)₄—SO₂—NH—SO₂-Ph-SO₃H (ortho)

1.36 g of 1, 2 benzenedisulfonyl anhydride, a synthesis of which can befound in J. Org. Chem., Vol. 48, No. 18, 1983, pg 2943-2949, was addedto a reaction vessel containing 48 g of a substantiallysulfonamide-functional polymer at 8.8% solids dissolved in dryacetonitrile, made according to the process of Example 1 using 812 EWpolymer. 2.1 g of triethylamine was then added the solution, mixed welland allowed to react overnight at room temperature. Solution NMR shows asignificant peak at −113.1 ppm which corresponds to the CF₂ groupadjacent to the sulfur in the pentafluorosulfonylimide of the polymer.1.1 g of 2M LiOH was then added, mixed well and the upper solution drieddown at 65 C to produce a clear, slight tan film of a PFSA with sidechains containing primarily a bissulfonylimide benzene-2 sulfonic group.Building a lower EW ionomer from a higher EW precursor polymer mayresult in higher backbone crystallinity at a given EW.

Example 11 Perfluorinated Polymer with Side Chains According to theFormula: —O—(CF₂)₄—SO₂—NH—SO₂-Ph-SO₃H (meta)

1.46 g of 1, 3 benzenedisulphonyl chloride (obtained from Lancaster inMorecambe, England) was added with 5 g of acetonitrile to 1.57 g of asubstantially sulfonamide-functional polymer at 10% solids dissolved inacetonitrile, made according to the process of Example 1 using 812 EWpolymer. 0.092 g of deionized water was then added and the containeremptied into a 3 neck flask, maintaining a nitrogen atmosphere. Thecontainer was rinsed with 3.5 g of acetonitrile and also added to theflask. Add 3 mls of triethyl amine to 17 ml of acetonitrile in anaddition funnel and slowly drip into the flask, over 3 hours, at roomtemperature. NMR of the solution shows a significant peak at −113.1 ppm.Add 2M LiOH solution to create a very basic solution, a brownprecipitate forms. Retain solid and rinse 3 times with acetonitrile.Rinse solids with 2M LiOH solution and then 5 times with deionizedwater. Rinse solid with 10% H2SO4/deionized water mixture to lower pH,followed by 5 DI water rinses. Add 15.8 g of methanol and dissolve solidwith modest heating. Rinse flask with 90/10 methanol/water mixture andrun everything through an ion exchange column of amberlite IR-120 beadstwice, diluting with 90/10 methanol/water mixture to help the flow. Drydown the polymer solution using nitrogen flow to create a film. Theresulting polymer had, by calculation, an EW of about 550, yet it wasprepared from a precursor polymer with an EW of 812. Building a lower EWionomer from a higher EW precursor polymer may result in higher backbonecrystallinity at a given EW.

Example 12-15 Prophetic

The polymers obtained in Examples 8 and 9 are sulfonated by reactionwith Na₂SO₃ to obtain acidic polymers with pendent disulfonated aromaticgroups bound via sulfonyl imide functions. The polymers obtained inExamples 10 and 11 are sulfonated by to obtain acidic polymers withpendent disulfonated aromatic groups bound via sulfonyl imide functions.The polymers so obtained are further sulfonated to obtain acidicpolymers with pendent polysulfonated aromatic groups bound via sulfonylimide functions.

Example 16 Proton Conductivity

Proton conductivity was measured using a standard, in-plane, 4 pointprobe conductivity apparatus with platinum electrodes, commerciallyavailable form Bekktech Inc., Loveland Colo. The cell was electricallyconnected to a potentiostat (Model 273, Princeton Applied Research) andan Impedance/Gain Phase Analyzer (SI 1260, Schlumberger). AC impedancemeasurements was performed using Zplot and Zview software (ScribnerAssociates). Temperature and relative humidity were controlled with aconstant humidity oven (TestEquity Model 1000H).

Conductivity was measured for the polymer of Example 10, the polymer ofExample 11 and a polymer of about 800 EW essentially similar to theprecursor polymer used to make the polymers of Examples 10 and 11. Thusall three polymers would be expected to have similar backbonecrystallinity, had the polymer backbone of a polymer with an EW of about800, however, the polymers of Examples 10 and 11 expected to have an EWof about 550 (by calculation). Conductivity was also measured for asimilar polymer of about 650 EW. The polymers of Examples 10 and 11showed improved conductivity at relative humidities of 50% or above. Atrelative humidities of 65% or higher, the polymers of Examples 10 and 11demonstrated conductivity comparable to the 650 EW polymer. At arelative humidity of 35%, the polymers of Examples 10 and 11demonstrated conductivity comparable to the 800 EW polymer. At arelative humidity of 50%, the polymers of Examples 10 and 11demonstrated conductivity intermediate between the 650 EW and 800 EWpolymers.

What is claimed is:
 1. A compound according to the formula:R¹ _(n)—Ar—SO₂NH—SO₂—R² wherein each R¹ is independently chosen from thegroup consisting of metal oxides, metal phosphates, metal phosphonatesand inorganic particles, wherein n is 1, 2 or 3, wherein Ar is anaromatic group which may include heterocycles and polycycles and may besubstituted, and wherein R² is a polymer.
 2. The compound according toclaim 1, wherein n is
 1. 3. The compound according to claim 1, wherein nis
 2. 4. The compound according to claim 1, wherein Ar is a phenyl. 5.The compound according to claim 1, wherein Ar is fluorinated.
 6. Thecompound according to claim 1, wherein Ar is perfluorinated.
 7. Thecompound to claim 1, comprising a perfluorinated backbone.
 8. Thecompound according to claim 1, wherein Ar is a first pendant group, andwherein the compound further comprises a second pendant group whichcomprises a group according to the formula: —SO₃H.
 9. The compoundaccording to claim 8, wherein the ratio of first to second pendantgroups is p, where p is between 0.01 and
 100. 10. The compound accordingto claim 8, wherein the ratio of first to second pendant groups is p,where p is between 0.1 and
 10. 11. The compound according to claim 8,wherein the ratio of first to second pendant groups is p, where p isbetween 0.1 and
 1. 12. The compound according to claim 8, wherein theratio of first to second pendant groups is p, where p is between 1 and10.
 13. A compound according to claim 1, wherein R¹ is chosen from thegroup consisting of metal phosphates and metal phosphonates.
 14. Apolymer electrolyte membrane comprising the compound according toclaim
 1. 15. The polymer electrolyte membrane according to claim 14additionally comprising a porous support.
 16. A polymer electrolytemembrane comprising the compound according to claim 14 aftercrosslinking.
 17. A fuel cell membrane electrode assembly comprising anelectrode comprising the compound according to claim 1.